Adult Patient Presenting with Spine Pain Following a Motor Vehicle Accident
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A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
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Neuromuscular Adverse Events Associated with Anti-PD-1 Monoclonal Antibodies
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Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
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A 38-Year-Old Man with Respiratory Failure and Progressive Leg Weakness
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Anti-HMGCR Autoantibodies in European Patients with Autoimmune Necrotizing Myopathies
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Focal Myopathy Mimicking Posterior Interosseous Nerve Syndrome
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The Neurologic Complications of Scleromyxedema
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Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
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Weak at the Knees
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Steroid-Responsive Myopathy with Deficient Chondroitin Sulfate C in Skeletal Muscle Conn Tissue
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Chloroquine Myopathy and Neuropathy with Elevated CSF Protein
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Hemiparetic Acute Myopathy of Intensive Care Progressing to Triplegia
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Erroneous Diagnosis Corrected After 28 Years
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Myasthenic Symptoms in Patients with Mitochondrial Myopathies
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A 59-Year-Old Man with Progressive Proximal Weakness Since Childhood
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A 54-year-old man with Dyspnea and Muscle Weakness
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Metabolic Lipid Muscle Disorders: Biomarkers and Treatment
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A 45-year-old man with Weakness and Myalgia after Orthopedic Surgery
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The Floppy Infant: Evaluation of Hypotonia
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Extension of the Clinical Spectrum of Danon Disease
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Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
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Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
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Clinical and Genetic Aspects of Distal Myopathies
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Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
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Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
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Cardiac Dysfunction in Neuromuscular Diseases
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Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
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Distal Myopathies:Clinical and Molecular Diagnosis and Classification
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Early Neurologic Complications Following Allogeneic Bone Marrow Transplant for Leukemia, a Prospective Study
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Proximal Myotonic Myopathy with MRI White Matter Abnormalities of the Brain
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X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma
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Various Types of Hereditary Inclusion Body Myopathies Map to Chromosome 9p1-q1
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Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
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Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
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Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
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Cerebral Involvement in McLeod Syndrome
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Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
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Tibial Muscular Dystrophy
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Molecular Genetics in Neurology
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